“…Currently, oxidative stress is researched by traditional indirect methods and is also explored in neurodegenerative diseases by evaluating products of lipid peroxidation (e.g., malondialdehyde [ 106 , 107 ] and 4-hydroxynonenal [ 108 ]), products of oxidized proteins (e.g., advanced oxidation protein products (AOPP)) [ 40 ], and by “comet assay”, an efficient tool to measure DNA breaks at the single-cell level [ 101 , 103 , 109 , 110 , 111 ]. Furthermore, direct methods of detection were adopted using confocal and live-cell imaging, flow cytometry, and/or HPLC methods (for more details, see Dikalov et al, 2014 [ 112 ]), enabling the investigation of the distinct participation of O 2 •− , H 2 O 2 and •OH/OONO •− species [ 40 , 101 , 102 , 103 , 113 , 114 , 115 , 116 , 117 , 118 ]. Since these assays show high analytical sensitivity and precision, indirect and direct methods are complementary tools to investigate possible therapeutic strategies against neurodegenerative diseases, as discussed later.…”